BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    *

    MDR report key: 2982150 · Received February 18, 2013

    Report

    Report Number
    2982150
    Event Type
    Malfunction
    Date Received
    February 18, 2013
    Date of Event
    October 31, 2012
    Report Date
    November 15, 2012
    Manufacturer
    ABBOTT LABORATORIES, INC.
    Product Code
    HQL
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    ND, US

    Narratives

    Description of Event or Problem · 1

    STICKLY LENS, UNABLE TO USE.WHAT WAS THE ORIGINAL INTENDED PROCEDURE?CATARACT EXTRACTION WITH IMPLANT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    70995 * LENS HQL ABBOTT LABORATORIES, INC. * *

    Patients

    Seq Age Sex Outcome Treatment
    1 *